首页> 外文OA文献 >THE ACTION OF SULFONAMIDES ON THE RESPIRATION OF BACTERIA AND YEAST : INHIBITION OF BACTERIAL AND YEAST CARBOXYLASES BY SULFONAMIDE DRUGS STRUCTURALLY RELATED TO COCARBOXYLASE
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THE ACTION OF SULFONAMIDES ON THE RESPIRATION OF BACTERIA AND YEAST : INHIBITION OF BACTERIAL AND YEAST CARBOXYLASES BY SULFONAMIDE DRUGS STRUCTURALLY RELATED TO COCARBOXYLASE

机译:磺酰胺类药物对细菌和酵母菌的呼吸作用:结构上与羧甲基化酶有关的磺酰胺类药物对细菌和酵母羧化酶的抑制作用

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摘要

The inhibiting effects of sulfonamide drugs and their derivatives on the anaerobic decarboxylation of pyruvic acid by Staphylococcus aureus, Escherichia coli, baker's and brewer's yeast, and a carboxylase preparation from brewer's yeast have been investigated. These drugs are: sulfanilamide, sulfapyridine, sulfadiazine, sulfamethyldiazine, sulfathiazole, sulfamethylthiazole, sulfanilamido-5-ethyl-4-thiazolone, 2-aminopyrimidine, 2-aminothiazole, and 2-aminopyridine. The sulfathiazole ring appears to exercise decidedly greater specific inhibiting effect on the carboxylases of Staph. aureus and E. coli. The inhibiting effect on yeast carboxylase is non-differentiable among all the substances tried, except sulfamethyldiazine which is completely ineffective on the carboxylases of the organisms studied. The specific inhibitory effect of sulfathiazole on the carboxylases of Staph. aureus and E. coli in comparison to sulfanilamide, sulfapyridine, and sulfadiazine is in harmony with in vivo and in vitro experimental results of other investigators. The results of the present investigation appear to support the hypothesis (1) that sulfonamides exert their bacteriostatic action through chemical affinity for the carrier proteins of certain respiratory enzymes of the bacterial cell, and that this affinity may in part be related to structural similarity between components of the drugs and the corresponding respiratory coenzymes.
机译:研究了磺胺类药物及其衍生物对金黄色葡萄球菌,大肠杆菌,面包酵母和啤酒酵母的丙酮酸厌氧脱羧的抑制作用,以及由啤酒酵母制备的羧化酶。这些药物是:磺胺,磺胺吡啶,磺胺嘧啶,磺胺甲基二嗪,磺胺噻唑,磺胺甲基噻唑,磺胺基氨基-5-乙基-4-噻唑酮,2-氨基嘧啶,2-氨基噻唑和2-氨基吡啶。巯基噻唑环似乎对金黄色葡萄球菌的羧基酶具有明显更大的特异性抑制作用。金黄色葡萄球菌和大肠杆菌。在所有尝试的物质中,对酵母羧化酶的抑制作用是不可区分的,只是磺胺甲基二嗪对研究的生物的羧化酶完全无效。磺胺噻唑对葡萄球菌羧化酶的特异性抑制作用。与磺胺,磺胺吡啶和磺胺嘧啶相比,金黄色葡萄球菌和大肠杆菌与其他研究者的体内和体外实验结果相吻合。本研究的结果似乎支持以下假设(1):磺酰胺通过对细菌细胞某些呼吸酶的载体蛋白的化学亲和力发挥其抑菌作用,并且这种亲和力可能部分与组分之间的结构相似性有关药物和相应的呼吸辅酶。

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